Variant (rsID / SNP)

rs201202764

rs201202764 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDK4. Location: chromosome 12, position 58,145,038. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CDK4Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:58145038
Cytoband: 12q14.1
HGVS: NM_000075.4(CDK4):c.306A>G (p.Thr102=)
Allele change: Synonymous_T102T

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Familial melanoma|Melanoma, cutaneous malignant, susceptibility to, 3

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.